Massive tumor study reveals rare genetic markers
NCT ID NCT04010240
First seen Oct 31, 2025 · Last updated May 01, 2026 · Updated 25 times
Summary
This study examined tumor samples from 3,820 people with advanced solid cancers to find how many had NTRK gene fusions. Researchers used genetic testing to identify these rare changes. The goal was to understand how common these fusions are, not to test a new treatment.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Institut Bergonié
Bordeaux, Aquitaine, 33000, France
Conditions
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